List of variants in gene SMAD4 reported as benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_005359.6(SMAD4):c.*11C>T	rs11663402	0.00538
NM_005359.6(SMAD4):c.354G>A (p.Ala118=)	rs145988618	0.00268
NM_005359.6(SMAD4):c.1573A>G (p.Ile525Val)	rs149755320	0.00071
NM_005359.6(SMAD4):c.*6522C>T	rs183472455	0.00047
NM_005359.6(SMAD4):c.*1067G>A	rs542839921	0.00005

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